Product Details

SNP ID
rs189381725
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:10490563 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTATCTTTCCCATCAATTAGTAT[A/G]ATGGGAAAATTCTTGTAGTGTTCGA
Phenotype
MIM: 611434
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CLNK PubMed Links

Gene Details

Gene
CLNK
Gene Name
cytokine dependent hematopoietic cell linker
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_052964.2 1559 Missense Mutation NP_443196.2
XM_011513775.2 1559 Missense Mutation XP_011512077.1
XM_017007684.1 1559 Intron XP_016863173.1
XM_017007685.1 1559 Intron XP_016863174.1

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